Primary Device ID | 35060206630179 |
NIH Device Record Key | a0a8f030-5e64-42bf-b0da-4d3531293d4a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CELOX EMS |
Version Model Number | FG08834281 |
Catalog Number | FG08834281 |
Company DUNS | 238476068 |
Company Name | MEDTRADE PRODUCTS LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk | |
Phone | +4401270500019 |
info@medtrade.co.uk |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Size Text, specify | 0 |
Length | 8 Inch |
Width | 8 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15060206630175 [Primary] |
GS1 | 35060206630179 [Package] Contains: 15060206630175 Package: Shelf Carton [5 Units] In Commercial Distribution |
GS1 | 75060206630177 [Package] Package: Shipper Case [50 Units] In Commercial Distribution |
FRO | Dressing, Wound, Drug |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-01 |
Device Publish Date | 2020-09-23 |
35060206630179 | Hemostatic Gauze Pad. The device is indicated for temporary external use to control moderate to |
35060206630162 | Hemostatic Gauze Pads: The device is indicated for: temporary external use to control moderate t |